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HRID 570127作成日:2026年10月26日

Potassium Carbonate → 6,6-difluoro-2-(4-fluorophenyl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine

https://huagongshe.com/reaction/570127

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2,2-Difluoropropane-1,3-diyl dimethanesulfonateHCID 242871—
反応物3-(4-fluorophenyl)-1H-pyrazol-5-olHCID 178515624—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物6,6-difluoro-2-(4-fluorophenyl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazineHCID 8948822956%

反応条件

温度60 °C

反応手順

To a solution of 3-(4-fluorophenyl)-1H-pyrazol-5-ol (4 g, 22.47 mmol) in DMF (30 mL) was added K2CO3 (12.4 g, 89.88 mmol) and 2,2-difluoropropane-1,3-diyl dimethanesulfonate (9 g, 33.7 mmol) at room temperature and then stirred for 16 h at 60° C. The progress of the reaction was monitored by TLC. Thereafter, the reaction mixture was diluted with cold water and extracted with diethyl ether. The organic layer was dried over anhydrous sodium sulphate and concentrated to get the crude product. Purification by column chromatography over silica gel (eluent 5-10% ethyl acetate in petrol ether) yielded 6,6-difluoro-2-(4-fluorophenyl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine (3.2 g, 56%) as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09023844B2
出典データセットuspto-grants-2015_05
ORD IDord-ca030abcf55f4cd2950e44fc900b0eee
出典メモuspto-grants-2015_05